| Literature DB >> 14515130 |
Xiao Fei Wang1, Chen Xi Zhou, Qi Xian Shi, Yu Ying Yuan, Mei Kuen Yu, Louis Chukwuemeka Ajonuma, Lok Sze Ho, Pui Shan Lo, Lai Ling Tsang, Yu Liu, Sun Yi Lam, Ling Nga Chan, Wen Chao Zhao, Yiu Wa Chung, Hsiao Chang Chan.
Abstract
Cystic fibrosis transmembrane conductance regulator (CFTR) is a cAMP-activated chloride channel expressed in a wide variety of epithelial cells, mutations of which are responsible for the hallmark defective chloride secretion observed in cystic fibrosis (CF). Although CFTR has been implicated in bicarbonate secretion, its ability to directly mediate bicarbonate secretion of any physiological significance has not been shown. We demonstrate here that endometrial epithelial cells possess a CFTR-mediated bicarbonate transport mechanism. Co-culture of sperm with endometrial cells treated with antisense oligonucleotide against CFTR, or with bicarbonate secretion-defective CF epithelial cells, resulted in lower sperm capacitation and egg-fertilizing ability. These results are consistent with a critical role of CFTR in controlling uterine bicarbonate secretion and the fertilizing capacity of sperm, providing a link between defective CFTR and lower female fertility in CF.Entities:
Mesh:
Substances:
Year: 2003 PMID: 14515130 DOI: 10.1038/ncb1047
Source DB: PubMed Journal: Nat Cell Biol ISSN: 1465-7392 Impact factor: 28.824